| HS Code | 787068 |
| Appearance | milky white liquid |
| Solid Content Percent | 55.0 |
| Viscosity Mpa S 25c | 1500 |
| Ph 25c | 4.5 |
| Glass Transition Temperature C | 0 |
| Minimum Film Forming Temperature C | 0 |
| Particle Size Micrometer | 0.5 |
| Film Appearance | transparent and flexible |
| Tensile Strength Mpa | 6.0 |
| Elongation At Break Percent | 800 |
As an accredited SUMIMKAFLEX S-755 VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | SUMIMKAFLEX S-755 VAE Emulsion is supplied in 200 kg drums or 1000 kg IBC totes, sealed and labeled for safe transport. |
| Container Loading (20′ FCL) | 20′ FCL: palletized drums/IBCs, stable loading, no DG restrictions, maximizing payload for SUMIKAFLEX S-755 VAE Emulsion. |
| Shipping | SUMIKAFLEX S-755 VAE Emulsion ships as a non-hazardous aqueous dispersion in drums, IBC totes, or tank trucks. Protect from freezing and extreme heat; ideal storage is 5–35°C. Ensure containers are sealed, upright, and well-ventilated. Standard shelf life is six months from manufacture with proper handling. |
| Storage | Store SUMIMKAFLEX S-755 VAE Emulsion in sealed, original containers in a cool, dry, well-ventilated area away from direct sunlight and heat sources. Maintain temperatures between 5°C and 35°C to prevent freezing or coagulation. Keep tightly closed when not in use, protect from moisture, and follow the Safety Data Sheet for shelf life and handling. |
| Shelf Life | Store at 5–35°C, avoid freezing. Shelf life is 6 months from manufacture date in original sealed container. |
A two-component, wood-flooring adhesive incorporating SUMIMKAFLEX S-755 as the primary binder meets D4 class moisture resistance when co-reacted with an emulsifiable diisocyanate prepolymer at 2.5–4.0 parts per hundred parts wet emulsion (phr). The mill-base is compounded under vacuum planetary mixing (e.g., Ross Double Planetary, 20–25 inHg vacuum) to entrain minimal air, consisting of 70–82 wt% of the S-755 emulsion (55% solids, MFFT approx. 2 °C), 12–25 wt% of a 1:1 blend of calcium carbonate and quartz flour (15 μm mean particle diameter), 0.2–0.4 wt% of an associative polyurethane thickener, and 0.1 wt% of a silicone-based defoamer. Tensile shear strength on beech after 6-hour boiling water cycle followed by 2-hour 60 °C drying exceeds 4.0 N/mm² when tested according to EN 204:2016 durability class D4, with cohesive wood failure routinely observed above 80%. Adhesive open time under 23 °C/50% RH remains workable at 45 minutes, measured by EN 14256:2007 spatula test. A production-scale bottleneck occurs during winter months when factory temperature drops below the MFFT of 2 °C; the film-formation lag manifests as micro-crazing on trowel ridges unless the slabs and adhesive are pre-conditioned at ≥8 °C for 12 hours before laying. Long-term water-immersion resistance is inferior to two-component epoxy systems, and the formulation must not be combined with amine-based epoxy accelerants due to rapid viscosity build-up and CO₂ bubble entrapment from isocyanate-water side reactions.
Continuous spray application of S-755 onto polyethylene nonwoven webs at coat weights of 1.8–2.5 g/m² achieves structural integrity in sanitary pads and infant diapers while maintaining air permeability. The emulsion is delivered through a narrow-pattern nozzle system (e.g., Nordson Control Coat with 0.25 mm orifices) at a fluid pressure of 0.8–1.2 bar and atomized with dry air at 0.5 bar, generating a spiral-spray footprint that avoids strike-through to the absorbent core. Wet-peel adhesion between SMS (spunbond-meltblown-spunbond) and PE backsheet, measured per WSP 401.1 at 0.0 N/25 mm withdrawal rate after 30-second open time, typically falls in the range of 0.25–0.45 N/25 mm, with cohesive failure within the adhesive layer indicating proper entanglement. The emulsion’s low-viscosity profile (300–600 mPa·s at 20 rpm Brookfield RVT spindle #3) minimizes nozzle clogging during start-stop cycles inherent in crescent-former machines. Compliance with OEKO-TEX Standard 100 Class I for infant articles is documented through gas chromatographic headspace analysis showing migrated monomeric vinyl acetate below the 5 μg/m² threshold per CSN EN 16729-1:2018. Processing engineers have noted that when relative humidity in the converting hall exceeds 70% RH, the dried film surface re-tackifies, leading to telescoping of jumbo reels; pre-drying of the substrate with infrared banks (30 kW output, 1.5 m length) at 90 °C surface temperature for 0.8 seconds eliminates this defect.
When S-755 is proportioned at a polymer-to-cement weight ratio of 0.10–0.15 in a two-component flexible cementitious waterproofing slurry, the cured membrane exhibits elongation at break exceeding 200% per GB/T 23445-2009 Type II and crack-bridging ability over a 0.75 mm dynamic crack measured at −10 °C per GB/T 50108-2008. The liquid component comprises 55–65 wt% S-755 emulsion, 0.3–0.5 wt% of a modified starch ether anti-sedimentation agent, 0.2 wt% of a blend of mineral oil and silicone defoamers, and the balance water to achieve a solids content of 28–32%. The powder component contains 42.5R ordinary Portland cement, 200-mesh quartz sand, and 3–5 wt% of a calcium lignosulfonate retarder to offset the rapid setting triggered by acetate ions in the emulsion. In forced-action paddle mixers (e.g., Collomix Xo 4R with 600 rpm rotor speed) the blend is mixed for 180 seconds, then applied in two coats by brush or notched trowel to a total dry thickness of 1.2–1.5 mm. A manufacturing pitfall arises when high-alumina cement is substituted into the powder due to exothermic flash setting, reducing pot life to less than 15 minutes; only ordinary Portland or pozzolanic-modified cements are compatible. Although the cured film passes 2,000-hour QUV-B accelerated weathering according to ISO 11507:2007, sustained exposure to UV without an acrylic topcoat results in gradual chalking and loss of elongation within 12 months in exterior horizontal applications.
A side-seaming adhesive for clay-coated solid bleached sulfate (SBS) folding cartons, natively resistant to condensation in chilled environments, is produced by compounding S-755 with glycerol ester of rosin at a weight ratio of 100:20 and a plasticizing level of triacetin at 4 phr. Adhesive viscosity is targeted at 450–550 mPa·s (Brookfield RVT, spindle #4, 20 rpm) to sustain clean transfer from the stack roller of a disc-type gluing station (e.g., Gietz FSA 700) at line speeds of 180–220 m/min. Peel adhesion of the bonded side-seam after 24-hour conditioning at 5 °C and 85% RH remains above 2.0 N/15 mm (TAPPI T 494 om-21), a performance threshold that rejects formulations based on homopolymer PVAc emulsions. Compliance with indirect food contact regulations under FDA 21 CFR 176.170 (Components of paper and paperboard in contact with aqueous and fatty foods) is documented via room-temperature total extraction testing per FDA 21 CFR 176.170(d)(1) and migration trials with food-simulating solvent 10% ethanol at 40 °C. Film-forming temperature limitations impose a minimum carton blank temperature of 5 °C before gluing; below this point, the latex fails to coalesce and the seam exhibits a paper-tear failure rate below 40% of the guaranteed bond strength. Cleaning protocols for the glue pot use warm water only, as isopropanol-based flushing agents prematurely destabilize the emulsion, causing irreversible grit formation visible as streaks on printed artwork.
Backcoating of woven upholstery fabric with S-755 at an add-on of 20–45 g/m² produces a high-friction, anti-fraying surface that locks the weft yarns without impairing the seam-slippage resistance required under BS EN ISO 13936-2:2004. The coating compound, consisting of 80–90 phr emulsion (55% solids), 10–20 phr fine ground calcite (D50 2 μm), and 0.3–0.5 phr ammonium stearate dispersion as a release aid, is applied by knife-over-roll coater with a gap setting of 0.2–0.3 mm and dried in a two-zone forced-air oven: zone 1 at 80 °C for 90 seconds, zone 2 at 130 °C for 120 seconds. Tensile strength retention in the warp direction after 5 home-laundering cycles (AATCC 135-2018, warm wash: 40 °C, tumble dry medium) averages 75–85% of the original value, while formaldehyde release according to GB 18401-2010 is not detectable (<16 mg/kg) due to the absence of N-methylol crosslinkers. Production-scale trials on a Brückner stenter with pin-and-clip chain reveal that misting and build-up on the coating knife occur when ambient humidity exceeds 65% RH; in-line dehumidification to 45–50% RH restores a clean edge profile. This backcoating is not recommended for fabrics destined for outdoor furniture or automotive seating, where plasticizer extraction by body oils causes progressive embrittlement and surface tack below 15 °C.
Substituting high-Tg styrene-butadiene latex with S-755 in the pre-coat layer of tufted automotive floor mats eliminates formaldehyde scavenger requirements and reduces total VOC emissions to <50 µgC/g under VDA 277. The compound is prepared in a high-shear dissolver (e.g., IKA LR-1000 with 80 mm Cowles blade at 3,000 rpm) by blending 45–50 parts dry S-755 emulsion (55% solids) with 50–55 parts calcium carbonate filler (10 μm) and 1.0 part of a naphthenic process oil; total solids target is 76–78%. The paste is applied to the non-pile side of a nylon 6,6 tufted polyester primary backing using a comma bar at a dry coating weight of 250–350 g/m² and cured in a forced-air tunnel at 140 °C for 8 minutes. Initial tuft-withdrawal force according to SAE J365 exceeds 9.0 N, but accelerated aging at 90 °C for 1,000 hours (ISO 188:2011, Method B) causes a 12–18% decay in pull strength, attributed to oxidative degradation of the ethylene segment in the VAE backbone. Designers therefore restrict this formulation to passenger-compartment floor carpets with a service-temperature cap of 80 °C, avoiding proximity to transmission tunnels. Adhesion to polyurethane foam laminated in a second step passes 5-cycle wet/dry peel per FMVSS 302 without after-flame, but the backing must not be stored in contact with uncured polyester resin components, which migrate through the primary backing and plasticize the S-755 film within 48 hours.
| Application Segment | S-755 Loading (Typical) | Key Performance Standard | Processing Equipment |
|---|---|---|---|
| D4 parquet adhesive | 70–82% wet weight | EN 204:2016 D4 | Vacuum planetary mixer |
| Hygienic nonwoven lamination | 1.8–2.5 g/m² dry | WSP 401.1, OEKO-TEX 100 Class I | High-speed spiral-spray applicator |
| Flexible cementitious waterproofing | polymer/cement ratio 0.10–0.15 | GB/T 23445-2009 Type II | Forced-action paddle mixer |
| Folding carton side-seam | 100 phr emulsion + 20 phr resin ester | FDA 21 CFR 176.170 | Disc-gluing station |
| Automotive carpet backcoating | 45–50 phr dry S-755 solids | SAE J365, VDA 277 | High-shear dissolver + comma bar |
| Upholstery backcoating | 20–45 g/m² dry add-on | BS EN ISO 13936-2:2004, GB 18401 | Knife-over-roll coater |
In powder-form interior wall putty (JG/T 298-2010 Type Y), replacing conventional polyvinyl alcohol colloid with a S-755 liquid component added on-site at 3%–5% by weight of dry powder significantly improves scratch adhesion and feathering properties. The field mixing procedure charges a heavy-duty drill-driven Jiffy mixer with 25 kg of a pre-blended dry mix (white Portland cement 15–20%, calcium carbonate 55–65%, talc 10–15%, hydroxyethyl methyl cellulose ether 0.3–0.5%, and sodium gluconate retarder 0.1%), to which S-755 diluted 1:1 with water is added under slow-speed (400 rpm) continuous mixing to achieve a target total water-to-solid ratio of 0.38–0.42. The resulting paste passes 150 μm wet-film sandability after 4 hours at 20 °C/60% RH and develops a bond strength to concrete substrate above 0.4 MPa (JG/T 298-2010, adhesive strength after water immersion) without the blistering commonly observed with re-dispersible powder-modified putties. Because S-755 acts as a continuous-film former, overcatalyzing with calcium formate accelerators must be limited to 0.5% of cement weight; exceedance leads to a dense skin that traps moisture and delaminates when overcoated with alkyd-based decorative paints. Under prolonged damp-substrate conditions (> 85% RH for 72 hours), the putty exhibits slight softening and a 15% drop in compressive strength; hence it is excluded from wet-room floor screeds and exterior EIFS base coats.
Ex-situ addition of S-755 to a C2TE/S2-class cementitious tile adhesive mix water (replacing 40% of the standard redispersible polymer powder) yields a slump-free mortar with ≥0.5 MPa tensile adhesion after water immersion (EN 12004:2007+A1:2012) and ≥0.4 MPa after heat ageing at 70 °C. The dry blend for a 1,000 kg batch comprises 350 kg ordinary Portland cement, 550 kg silica sand (0.1–0.5 mm), 30 kg of a water-retaining cellulose ether, 15 kg polycarboxylate superplasticizer powder, and 55 kg of a vinyl acetate-ethylene redispersible powder; the liquid component at the point of application is composed of 6.5 kg S-755 emulsion (55% solids) mixed with 10.5 kg water per 100 kg dry powder. Mortar prepared in an orbital-plaster mixer (e.g., PFT HM 5) exhibits an extended open time of 40 minutes (EN 1346) and a transverse deformation of ≥5.0 mm (EN 12002) when tested on polyethylene film. In practice, long pot-life stability is correlated with the pH of the blended water: at a pH below 9.5, the acetate groups in S-755 undergo slow hydrolysis, liberating acetic acid that depresses hydration of C3A phases and postpones final set by 3–4 hours; this effect is mitigated by adjusting the retarder package. Segregation of the liquid component in the tank before mixing is a documented field failure mode—reciprocating air-operated diaphragm pumps with a 1:1 ratio and 15 mm port size have been retrofitted with re-circulation loops to maintain homogeneity over shifts exceeding 8 hours. The final adhesive complies with the low VOC emission class A+ (<1,000 μg/m³ after 28 days) of ISO 16000-9:2006.
| Regulatory/Compliance Standard | Application Area | Measured Parameter | S-755 Contribution / Condition |
|---|---|---|---|
| EN 204:2016 D4 | Wood flooring adhesive | Wet shear strength after boil cycle | ≥ 4.0 N/mm² with co-reactant isocyanate |
| OEKO-TEX Standard 100 Class I | Hygienic nonwoven | Vinyl acetate migration | < 5 μg/m² |
| FDA 21 CFR 176.170 | Folding carton adhesive | Total extractives in food simulants | Passes water/10% ethanol at 40 °C |
| GB/T 23445-2009 Type II | Cementitious waterproofing | Elongation at break, % | ≥ 200% |
| VDA 277 | Automotive carpet | TVOC emission | < 50 µgC/g |
| EN 12004:2007+A1 C2S2 | Tile adhesive | Tensile adhesion after water immersion | ≥ 0.5 MPa |
| JG/T 298-2010 Type Y | Wall putty | Adhesive strength after water immersion | ≥ 0.4 MPa |
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In adhesive formulations for paper and packaging, the selection of a base emulsion governs both the application rheology and the mechanical resilience of the bonded joint. SUMIKAFLEX S-755, a vinyl acetate-ethylene (VAE) copolymer dispersion stabilized by a poly(vinyl alcohol) protective colloid, is engineered for high-speed converting operations where rapid setting and broad substrate adhesion are required. The product is supplied at a nominal solids content of 55% w/w and a Brookfield LV viscosity of 3,500 mPa·s (spindle #3, 30 rpm, 25°C, ISO 2555). Its pH falls within 4.0–5.0 (ISO 976), and the minimum film-forming temperature (MFFT) measured on a gradient bar per ISO 2115 is 0°C, correlating with a glass transition temperature (Tg) of approximately 0°C determined by differential scanning calorimetry at 10 K/min (ISO 11357-2). The particle size, determined by laser diffraction (ISO 13320), lies in the submicron range, producing films with a milky appearance that clarifies upon complete water evaporation.
Unlike poly(vinyl alcohol)-stabilized VAE emulsions of lower ethylene content such as SUMIKAFLEX S-752, S-755 incorporates a higher molar fraction of ethylene in the copolymer backbone. This compositional shift depresses the Tg into the ambient range without the need for coalescing solvents, yielding a balance of cohesive strength and elongation at break that exceeds 700% (ASTM D882, 0.5 mm dry film thickness, 500 mm/min crosshead speed). The absence of external plasticizers eliminates migratory species that can compromise food-contact compliance or cause blocking in stacked substrates.
Within the Sumikaflex portfolio, S-755 occupies a mid-range position defined by its ethylene content and resulting flexibility. A structured comparison with adjacent grades clarifies the product’s design envelope.
| Property | SUMIKAFLEX S-752 | SUMIKAFLEX S-755 | SUMIKAFLEX S-408 |
|---|---|---|---|
| Solids content (% w/w) | 54–56 | 54–56 | 54–56 |
| Brookfield LV viscosity (mPa·s, #3, 30 rpm, 25°C) | 2,000–3,000 | 3,000–5,000 | 1,000–2,000 |
| Tg (DSC midpoint, °C) | approx. +5 | approx. 0 | approx. -15 |
| MFFT (°C, ISO 2115) | +5 | 0 | -15 |
| Tensile strength (MPa, ASTM D882) | 7.0–9.0 | 4.5–6.5 | 1.5–3.0 |
| Elongation at break (%) | 400–600 | 700–900 | 1,200–1,500 |
S-755 delivers intermediate flexibility with higher elongation than S-752 while maintaining roughly twice the tensile strength of the ultra-flexible S-408. This profile suits applications where the bondline must absorb stress without cohesive failure, such as semi-automated carton sealing on lines that stack product immediately after compression.
The film formation mechanism of S-755 relies on the plastifying effect of the ethylene segments within the copolymer, reducing the minimum film-forming temperature to 0°C. At ambient temperatures above 15°C, complete interdiffusion of polymer particles occurs without coalescing aids, yielding a clear, continuous film. This characteristic is advantageous in closed-loop machine application where volatile organic compounds (VOC) from coalescent agents would accumulate in recirculated adhesive troughs. However, at processing temperatures below 5°C, the coalescence rate slows markedly, and an open time exceeding 30 seconds can result in a drastic loss of tack prior to compression. In cold-plant environments, pre-warming the emulsion to 20°C–25°C and keeping the glue station insulated is necessary to maintain consistent film formation and bond strength.
Despite its flexibility, the film of S-755 exhibits pronounced water whitening when immersed in water at 23°C for 24 h (EN 204 condition), which causes a reversible loss of clarity and a reduction in wet cohesive strength to approximately 30% of the dry value. This behavior constrains the use of the unmodified emulsion in exterior or high-humidity packaging unless a reactive crosslinker is incorporated.
When formulated as a one-component waterborne laminating adhesive for biaxially oriented polypropylene (BOPP) / paper composites, a key bottleneck arises from the insufficient anchorage on untreated film surfaces. The surface energy of corona-treated BOPP must be maintained at a minimum of 38 mN/m (ASTM D2578) immediately before coating; a drop to 34 mN/m due to aging can reduce peel strength by more than 50%. A typical process configuration on a roll-fed laminator employs a three-roll metering system applying 5–8 g/m² dry weight at line speeds of 80–150 m/min. The coated web passes through a tunnel oven set at 85°C with a residence time of 25–35 s, followed by nip lamination at 0.3 MPa linear pressure and 110°C roll temperature. Adhesion failures traced to heat-seal initiation lag were mitigated by raising the laminator nip temperature to 115°C; however, this narrows the safe window for heat-sensitive BOPP films that shrink at temperatures above 120°C.Co-formulation of S-755 with borax-modified dextrin solutions for paper tube winding introduces a distinct rheological risk. The poly(vinyl alcohol) protective colloid complexes with borate ions, causing a sharp stepwise increase in viscosity. In pilot trials on a high-speed spiral tube winder (line speed 60 m/min), addition of a 7% borax-dextrin solution to the emulsion at a ratio of 20:80 (wet weight) elevated the mixture viscosity from 4,200 mPa·s to beyond 30,000 mPa·s within 60 seconds, leading to pump cavitation and streaking on the bondline. Successful blending requires metering the dextrin solution into the emulsion under high-turbulence in-line mixing, limiting the borax concentration to below 0.3% of total formulation weight, and verifying viscosity stability over a 4-hour pot-life cycle. When these constraints are observed, the hybrid adhesive achieves an initial wet tack sufficient to hold 3-ply kraft core layers at a winding angle of 54° without telescoping.
Dynamic surface tension governs the wetting behavior of S-755 on semi-porous substrates such as clay-coated board. Measurements using a bubble pressure tensiometer (Krüss BP100, range 50–5,000 ms) show that at a surface age of 100 ms, the dynamic surface tension is approximately 45 mN/m. This value is sufficiently low to spread uniformly on substrates with contact angles below 60°. However, on heavily coated board with a surface energy of 35 mN/m, retraction of the adhesive from the surface results in a cratered application pattern unless a nonionic surfactant of low HLB (4–6) is post-added at 0.05–0.1% on wet weight. Overdosing beyond 0.2% causes excessive foam generation in the recirculating reservoir, and a silicone-free defoamer at 0.02% must then be incorporated. This delicate balance is typical of VAE emulsions that lack the inherent low-surface-tension character of all-acrylic lattices.For foil-laminated packaging structures, S-755 serves as the primer coat that is subsequently heat-sealed against a polyethylene extrusion layer. The heat seal initiation temperature (HSIT) of the dry adhesive film lies between 80°C and 90°C, as measured by a gradient heat sealer at 0.5 N/mm² seal pressure and 1.5 s dwell time, according to ASTM F2029. The optimal seal bar temperature range is 110°C–130°C. Below 105°C, the peel strength on aluminum foil (EN 868-2 method) remains below the critical 2.5 N/15 mm threshold required for chevron peel pouch integrity. Above 135°C, thermal degradation of the adhesive manifests as blistering and a rapid drop in bond strength to less than 1.0 N/15 mm. Comparison with a lower-ethylene VAE (S-752) reveals that S-755’s lower Tg shifts the HSIT downward by approximately 5–8°C, widening the process window in machines with temperature gradients across the seal bar.
| Adhesive specification | Substrate system | T-peel strength (N/15 mm) | Lap shear (MPa) | Conditioning / Standard |
|---|---|---|---|---|
| S-755 (unmodified) | kraft/kraft, 20 g/m² coat | 3.8 (±0.4) | 2.1 (±0.3) | ISO 4587:2003, beech wood, 0.5 mm bondline, 7 d at 23°C/50% RH |
| S-755 + crosslinker (glyoxal 0.5% w/w on solids) | birch/birch, EN 205 | — | 4.6 (±0.5) dry / 2.7 (±0.3) after 4 h boil (EN 204 D2) | DIN EN 204 |
| S-755 + rosin ester tackifier 15% on solids | corona-treated BOPP/paper | 5.2 (±0.6) | — | Peel T-peel at 300 mm/min, 24 h at 23°C |
To overcome the intrinsic water sensitivity of the PVA-stabilized VAE matrix, a post-addition of water-dispersible blocked isocyanate crosslinker can be made. At an addition level of 1.5% active isocyanate on total emulsion solids, the pot life at 25°C extends to approximately 6 hours, as tracked by a doubling of the initial viscosity. The system deblocks during thermal drying (minimum 90°C for 3 minutes), curing over 7 days at ambient humidity (ISO 291 class 2). This approach elevates the bond durability to EN 204 D2 class, withstanding a 4-hour boiling water soak and redrying cycle while retaining at least 2.5 MPa lap shear. However, the isocyanate adduct must be mixed into the emulsion using a high-shear disperser (rotor-stator tip speed 15 m/s) to avoid local gelation due to rapid reaction with hydroxyl groups on the PVA stabilizer. Aged films demonstrate a substantial reduction in water whitening: submersion for 24 h at 23°C yields only a haze increase of 5% (ASTM D1003) versus 35% for the unmodified control. This upgrade path positions S-755 as a viable binder for exterior packaging applications where occasional moisture exposure is anticipated, without sacrificing the room-temperature coalescence that distinguishes it from harder VAE grades.